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pmid:36211815

Identifying a 6-Gene Prognostic Signature for Lung Adenocarcinoma Based on Copy Number Variation and Gene Expression Data.

Yisheng Huang · Liling Qiu · Xiaoye Liang · Jing Zhao · Haoting Chen · Zhiqiang Luo · Wanzhen Li · Xiaohua Lin · Jingjie Jin · Jian Huang · Gong Zhang

Oxidative medicine and cellular longevity · 2022 doi:10.1155/2022/6962163

Paper

complete

Experiment

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Data

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Analysis

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title
Identifying a 6-Gene Prognostic Signature for Lung Adenocarcinoma Based on Copy Number Variation and Gene Expression Data.
doi
10.1155/2022/6962163
pmid
36211815
authors array · 11 items
[0]
Yisheng Huang
[1]
Liling Qiu
[2]
Xiaoye Liang
[3]
Jing Zhao
[4]
Haoting Chen
[5]
Zhiqiang Luo
[6]
Wanzhen Li
[7]
Xiaohua Lin
[8]
Jingjie Jin
[9]
Jian Huang
[10]
Gong Zhang
journal
Oxidative medicine and cellular longevity
year
2022
abstract
The occurrence of lung adenocarcinoma (LUAD) is a complicated process, involving the genetic and epigenetic changes of proto-oncogenes and oncogenes. The objective of this study was to establish new predictive signatures of lung adenocarcinoma based on copy number variations (CNVs) and gene expression data. Next-generation sequencing was implemented to obtain gene expression and CNV information. According to univariate, multivariate survival Cox regression analysis, and LASSO analysis, the expression profiles of lung adenocarcinoma patients were screened and a risk score formula was established and experimentally validated in a local cohort. The model was evaluated by three independent cohorts (TCGA-LUAD, GSE31210, and GSE30219), and then validated by clinical samples from LUAD patients. A total of 844 CNV-related differentially expressed genes (CNV-related DEGs) were identified. These genes are significantly associated with the imbalance of various oxidative stress pathways. A CNV-associated-six gene signature was dramatically linked to overall survival in lung adenocarcinoma samples from both training and validation groups. Functional enrichment analysis further revealed involvement of genes in p53 signaling pathway and cell cycle as well as the mismatch repair pathway. Risk score is an independent marker considering clinical parameters and had better prediction in clinical subpopulation. The same signature also classified tumor tissues of clinical patients with CNV detected from their corresponding nontumorous tissues with an accuracy of 0.92. In conclusion, we identified a new class of 6 CNV-related gene markers that may act as efficient prognostic predictors of lung adenocarcinoma, thus contributing to individualized treatment decisions in patients.
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A univariate Cox proportional hazard regression model was conducted for each DEGs (844 genes) using the R package survival coxph function in training dataset with p < 0.01.
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The six-gene CNV-related signature classified clinical tumor tissues with detected CNVs from their corresponding adjacent nontumorous tissues with an accuracy of 0.92.
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The same signature also classified tumor tissues of clinical patients with CNV detected from their corresponding nontumorous tissues with an accuracy of 0.92.
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The six-gene CNV-related signature classified clinical tumor tissues with detected CNVs from their corresponding adjacent nontumorous tissues with an accuracy of 0.92.
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Characterization of a new genetic signature associated with copy number variation that determines outcome in lung adenocarcinoma patients
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null
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570
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Homo sapiens
title
Gene expression data for pathological stage I-II lung adenocarcinomas
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2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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[4]
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[5]
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A univariate Cox proportional hazard regression model was conducted for each DEGs (844 genes) using the R package survival coxph function in training dataset with p < 0.01.
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[0]
The transcriptome sequencing data was uploaded to the Gene Express Omnibus (GEO) database under the accession GSE197346. To review GEO accession GSE197346, go to https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE197346. Enter token cbmvowqorlclfcj into the box.
basis
The paper names GSE31210, GSE30219, GSE197346 in Gene Expression Omnibus (GEO) database and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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minimax
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GEO GSE197346
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36211815", "kind": "science-record", "revision": 4, "content_hash": "sha256:80ef91fb8b8298b68083d1089744942b5c38e4213e4548f1304359ce388211f9", "created_at": "2026-11-01T18:15:32Z", "updated_at": "2026-11-01T22:07:45Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identifying a 6-Gene Prognostic Signature for Lung Adenocarcinoma Based on Copy Number Variation and Gene Expression Data.", "doi": "10.1155/2022/6962163", "pmid": "36211815", "authors": ["Yisheng Huang", "Liling Qiu", "Xiaoye Liang", "Jing Zhao", "Haoting Chen", "Zhiqiang Luo", "Wanzhen Li", "Xiaohua Lin", "Jingjie Jin", "Jian Huang", "Gong Zhang"], "journal": "Oxidative medicine and cellular longevity", "year": 2022, "abstract": "The occurrence of lung adenocarcinoma (LUAD) is a complicated process, involving the genetic and epigenetic changes of proto-oncogenes and oncogenes. The objective of this study was to establish new predictive signatures of lung adenocarcinoma based on copy number variations (CNVs) and gene expression data. Next-generation sequencing was implemented to obtain gene expression and CNV information. According to univariate, multivariate survival Cox regression analysis, and LASSO analysis, the expression profiles of lung adenocarcinoma patients were screened and a risk score formula was established and experimentally validated in a local cohort. The model was evaluated by three independent cohorts (TCGA-LUAD, GSE31210, and GSE30219), and then validated by clinical samples from LUAD patients. A total of 844 CNV-related differentially expressed genes (CNV-related DEGs) were identified. These genes are significantly associated with the imbalance of various oxidative stress pathways. A CNV-associated-six gene signature was dramatically linked to overall survival in lung adenocarcinoma samples from both training and validation groups. Functional enrichment analysis further revealed involvement of genes in p53 signaling pathway and cell cycle as well as the mismatch repair pathway. Risk score is an independent marker considering clinical parameters and had better prediction in clinical subpopulation. The same signature also classified tumor tissues of clinical patients with CNV detected from their corresponding nontumorous tissues with an accuracy of 0.92. In conclusion, we identified a new class of 6 CNV-related gene markers that may act as efficient prognostic predictors of lung adenocarcinoma, thus contributing to individualized treatment decisions in patients.", "claims": [{"id": "claim-method", "statement": "A univariate Cox proportional hazard regression model was conducted for each DEGs (844 genes) using the R package survival coxph function in training dataset with p < 0.01.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36211815", "locator": "sections[7] \"2.5. 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